| Tag | Content |
|---|
EnhancerAtlas ID | HS042-03146 | Organism | Homo sapiens | Tissue/cell | Fetal_brain | Coordinate | chr1:178454600-178457240 | TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| SREBF1 | MA0595.1 | chr1:178455277-178455287 | ATCACCCCAC | + | 6.02 |
| | | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
| | | Number: 2 | ID | Chromosome | Start | End |
| GH01I178486 | chr1 | 178455536 | 178456535 | | GH01I178485 | chr1 | 178454417 | 178455199 |
| Enhancer Sequence | TCTGCCAGGA AGAACTTTCT GTACTTTTCT GCCAGATGAA ATCCTCCATT GTTACACCTT 60
CTATCCTATT ACCACCTTCC AGGCAGAAGG AAATGAATTG CTTTCCTGCC ACAGCTCTTG 120
GTTCACACTT CTGGTGCAGC ATTTTCCAAA CCGTCCTGAC TGTCTCCGTT AGTTCCTATG 180
AGACCATGTG CTTCTAAAAA CAGGAAACAG CCCTGCTCAT CTTGGTATCC ACAGTTCAAT 240
GCCTTCTTCA AAACAAGTAC TCAGGAAATT ATCGTCCAAT TAAATCATCT ACCAATGTGC 300
ACTATCCTAG TCCCCAGAGA GATACAAAGA AGTACAGAAC AGCCCCTGCC CTGTGAGATT 360
CTGCAATCTC AATAATTCAT AATTGTAATC ATTTATGATT AATAAAATGA GAATGAGGCC 420
AGCTCCATCT ATTAAGGAGA GAGGTGGGAG AAGGAGTGAG TCACTAAACA TTTCACTAGA 480
GAACTGAGAT TAAAATGGTA ATAACTACCA TTTATTGAGT GTCTGCCAGA TGCCAGGCAC 540
TGAGAGATGA GAAAAATAAG GTTCAGAGAA GTTAGGAAAC TTGCATAAGG CCACACAGTA 600
GGTACTGGAG CCAATATTCC AACTCTTGAC TGTCAGACTC TTGCTTTTAG AACCAAAATG 660
GATTATTTCT CCCCCAGATC ACCCCACTTC ACCTCCATTT CCATCCTAAA TTACCCAGGG 720
AGGACGAGAC AGTGAGCTGG CTCTGGCCAG ACAGGACCCC TGTAGGATGC GCTGGAATGC 780
AGCCGGAGTG GGGAGACTGT GGCCCAGCAC ACAACGCGCC CACACCACAC CCCACCTCTC 840
ATCCTCAACT CCCTGGCCTG CACCCTACTC ATGGAAGCCA GGCCTGGTCG CCCCAAGAGA 900
GGAACTCCCC AAGATGCTTG GGCCTGCCTG GGGTGGAGGT CCTAATTTCC AGCGACGCAG 960
ACAGGCACCT GTTTGGGGCC CTGGCCAGCT CCCAGCTGCC TCTGGGCGGG TGTCTTGGCT 1020
CAGGGCTGCA GAGTCAGGGG GTGCAGTTGT CCTCTGGGTC ACGGCTGGGC TCCCTAAGCC 1080
AAATGAGTCC GAGATGCTTT CTTTGGTCCC CAGAGAGCTC CCTTGAGCCT GGGAGCCGAG 1140
GCCCCGGCTG GATGTGGCAG ACCCAGGGGG TGCTGCTATC CTGGGAGTAG CTGGGGCATC 1200
GCGGGTGGCA TCGAGTGTGG GGCTCGAAGC GGAGGCCAGA AGAGTCGCAG TTACTTCCTG 1260
GGGGACAGAG AGGCTCCCCC GAGAGGCCGC AGCAGGGCTG GAGGGCTGGG ACGCCGAGGG 1320
CGCAGGGTGG GAAGACGCAC TCTGGGCAGT GACCGGCGGC ATCCTGGGTC CTTCCGCGGG 1380
AACCAAGGTG CCCCCCGGGG CCGCGAGGTT GGCCGAAGGG CCGGGTGTTA CCGCCCCTTG 1440
GGGCTGGAGG GCCGCTGGGC CCGCGGAGGC GGAAGCGCGC GAGTAGGAGG TGCGGAGGTC 1500
GGGCTCGCGG GGCTCCGGGC TGCCCCTCTG AGTGAGCCGC GCTGCTGAAG CCGGGCCCTG 1560
CGAGGCGCCC ACGGGGCCGG TGCTGGTCCC TAGGGCCAGA GAGAAGACTT CTGTGGGGTC 1620
CGCTGCGCCC GGGACCCCTC CCAAAGCCGA GGGCAAGAAG GAGTGGCTTC GCGCGCTGGC 1680
TCCCCGGGCC TGTGCCTCTT CCACGCCTGG CCTTGCCCAC CCAGTGCAGA CAGGGGCGAG 1740
CAGGGAGGGC CTCCTGAACC CAATAGCGCG GCCCAGGTGG CCAGCGAGCC TGGGGCAGCC 1800
AGGCAGGTGC CAGGATAGAC CTTAGATGAG AAGACAGGCT GTTACCCAGC TTCTGACCCA 1860
AATCTGATCA CAGCTACCAG CCTGGGCTCT GTCGCCTTCA GGGTGAGGTC CCTTAGTGAC 1920
TCACAGGGGG CCCGGCCGGC AGGATCTGGG CTCCCACACT CTCCAGCGCT GACTGTCCCC 1980
ACCCCACCTG CAGCTCCTTC CATCTGCAGT CCTCACCCAG CCACGCACCC CCACTCCACT 2040
TTGCAAGCTA AATCCTTCTC ATCCTTCCAA TAGTTATAAA GTCACCTCCT CTGCGAAATC 2100
CCCTGGACAA TTACAGGGGG GGATGCTCCC CTTCTCAGCG TCCCCACCAC GCCTGTGCCT 2160
ATACCAAGCA CCAGCCTCTT CCCAACTGGC TGTGAGCGCC TTCAGAACAA ACCTTCCCTT 2220
TTCGTTGTGT CCCCAAAATC TTGCCTGGTG GCTGTGCCTG GGCTAGCACA GGACTCCATC 2280
CACACTTTCT AATGAGTGAA TGAACGAGGC TCTGCTCGAC CTTGATCAAG TGCCCTCACT 2340
TTTCTGTGTC CTCAAAAAAA GACAATAATC CCTTTGTGTG ATATAGGAAT CTGTAAGGAG 2400
GCCAGGAAAA CGGTGATTTT GCCCTCAATT ACTCTAGTTA GCCTCAGAAC TCTTGGGAAG 2460
TAAAATGAGG TAACAGCTGT GAAGATGTTT CAGAAATTTT AAAATGCTAT AGGAATGCTG 2520
TCACTGTCCT TCCCAGCCAC CTCCCCATAC ATAATGCCAA CAGCTCATCA TCCCTCATCC 2580
TCTCCCTGCA GAGGAGCCTG CAATTCCGAG GGACTTTGCG GTGCTTCCCT CTGGATGCTG 2640
|
| |
|
|
|
